importScSeqScore.Rd
Plot single cell RNAseq data as heatmap track for Seurat object.
importScSeqScore(
object,
files,
samplenames,
...,
txdb,
gene,
id,
idents,
gr,
color,
withCoverageTrack = TRUE,
flag = scanBamFlag(isSecondaryAlignment = FALSE, isUnmappedQuery = FALSE,
isNotPassingQualityControls = FALSE, isSupplementaryAlignment = FALSE)
)
Seurat object.
bam file to be scanned.
sample names for files.
parameters used by readGAlignmentsList or readGAlignments
TxDb object for gene model.
Gene name to plot. (row value)
The id of gene used in txdb.
indentity class to define the groups to plot. (column value)
GRanges object to define the ploting region.
vector of colors used in heatmap.
plot coverage track or not.
An integer(2) vector used to filter reads based on their 'flag' entry.
if (FALSE) { # \dontrun{
library(TxDb.Hsapiens.UCSC.hg19.knownGene)
test_file <- "https://github.com/10XGenomics/subset-bam/raw/master/test/test.bam"
trs <- importScSeqScore(files=test_file,
txdb=TxDb.Hsapiens.UCSC.hg19.knownGene,
id="653635", gene = "WASH7P")
} # }